Mutation analysis of TMC1 identifies four new mutations and suggests an additional deafness gene at loci DFNA36 and DFNB7/11
Hilgert, N, Alasti, F, Dieltjens, N, Pawlik, B, Wollnik, B, Uyguner, O, Delmaghani, S, Weil, D, Petit, C, Danis, E, Yang, T, Pandelia, E, Petersen, MB, Goossens, D, Favero, JD, Sanati, MH, Smith, RJH, Van Camp, G
Published in Clinical genetics (01.09.2008)
Published in Clinical genetics (01.09.2008)
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Two modelling approaches of winemaking: first principle and metabolic engineering
Charnomordic, B., David, R., Dochain, D., Hilgert, N., Mouret, J.-R., Sablayrolles, J.-M., Vande Wouwer, A.
Published in Mathematical and computer modelling of dynamical systems (08.12.2010)
Published in Mathematical and computer modelling of dynamical systems (08.12.2010)
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Recursos tróficos utilizados por Plebeia intermedia (Apidae, Meliponini) en la localidad de Baritú, Salta, Argentina. Caracterización botánica de sus mieles
Flores, F. F., Lupo, L. C., Hilgert, N. I.
Published in Boletín de la Sociedad Argentina de Botánica (14.12.2015)
Published in Boletín de la Sociedad Argentina de Botánica (14.12.2015)
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A New Autosomal Recessive Form of Stickler Syndrome Is Caused by a Mutation in the COL9A1 Gene
Van Camp, Guy, Snoeckx, Rikkert L., Hilgert, Nele, van den Ende, Jenneke, Fukuoka, Hisakumi, Wagatsuma, Michio, Suzuki, Hiroaki, Erica Smets, R.M., Vanhoenacker, Filip, Declau, Frank, Van De Heyning, Paul, Usami, Shin-ichi
Published in American journal of human genetics (01.09.2006)
Published in American journal of human genetics (01.09.2006)
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Journal Article
A new locus for otosclerosis, OTSC8, maps to the pericentromeric region of chromosome 9
Bel Hadj Ali, Insaf, Thys, Melissa, Beltaief, Najeh, Schrauwen, Isabelle, Hilgert, Nele, Vanderstraeten, Kathleen, Dieltjens, Nele, Mnif, Emna, Hachicha, Slah, Besbes, Ghazi, Ben Arab, Saïda, Van Camp, Guy
Published in Human genetics (01.04.2008)
Published in Human genetics (01.04.2008)
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Amino acid 572 in TMC1: hot spot or critical functional residue for dominant mutations causing hearing impairment
Hilgert, Nele, Monahan, Kelly, Kurima, Kiyoto, Li, Cindy, Friedman, Rick A, Griffith, Andrew J, Van Camp, Guy
Published in Journal of human genetics (01.03.2009)
Published in Journal of human genetics (01.03.2009)
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